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      Externally controlled atom transfer radical polymerization

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          Abstract

          ATRP can be externally controlled by electrical current, light, mechanical forces and various chemical reducing agents. The mechanistic aspects and preparation of polymers with complex functional architectures and their applications are critically reviewed.

          Abstract

          Spatial and temporal regulations of ATRP by external stimuli are presented. Various ATRP techniques, eATRP, photoATRP, and mechanoATRP, are controlled by electrical current, light, and mechanical forces, respectively. Conversely, ARGET and SARA ATRP are controlled by chemical reducing agents. ICAR ATRP is a thermally regulated process through decomposition of a radical initiator. The aim of this review is to highlight the use of external regulations in ATRP and to summarize the state-of-the-art and future perspectives, focusing on mechanistic aspects, synthetic procedures, preparation of polymers with complex architectures and functional materials, and their applications.

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          Most cited references332

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          Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.

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            On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. I

            R Marcus (1956)
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              Merging photoredox catalysis with organocatalysis: the direct asymmetric alkylation of aldehydes.

              Photoredox catalysis and organocatalysis represent two powerful fields of molecule activation that have found widespread application in the areas of inorganic and organic chemistry, respectively. We merged these two catalysis fields to solve problems in asymmetric chemical synthesis. Specifically, the enantioselective intermolecular alpha-alkylation of aldehydes has been accomplished using an interwoven activation pathway that combines both the photoredox catalyst Ru(bpy)3Cl2 (where bpy is 2,2'-bipyridine) and an imidazolidinone organocatalyst. This broadly applicable, yet previously elusive, alkylation reaction is now highly enantioselective and operationally trivial.
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                Author and article information

                Journal
                CSRVBR
                Chemical Society Reviews
                Chem. Soc. Rev.
                Royal Society of Chemistry (RSC)
                0306-0012
                1460-4744
                2018
                2018
                : 47
                : 14
                : 5457-5490
                Affiliations
                [1 ]State Key Laboratory of Molecular Engineering of Polymers
                [2 ]Department of Macromolecular Science
                [3 ]Fudan University
                [4 ]Shanghai 200433
                [5 ]China
                [6 ]Department of Chemistry
                [7 ]Carnegie Mellon University
                [8 ]Pittsburgh
                [9 ]USA
                Article
                10.1039/C8CS00259B
                29868657
                2f216a7e-3e94-4a09-826b-41b33a391b1b
                © 2018

                Free to read

                http://rsc.li/journals-terms-of-use#chorus

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